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NCT06335823 · ClinicalTrials.gov registry record · NA
Efficacy of Transcutaneous Electrical Nerve Stimulation (TENS) for Pain Reduction During Intrauterine Device (IUD) Insertion in Outpatient Gynecology
A NA study, sponsored by University Hospitals Cleveland Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 60
- Enrollment target
NCT06335823: Completed NA study, sponsored by University Hospitals Cleveland Medical Center.
NCT06335823 is a NA study that has completed, run by University Hospitals Cleveland Medical Center. The registered enrollment target is 60 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06335823, a NA study, has completed, sponsored by University Hospitals Cleveland Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 60 participants
- Enrollment target
Study Summary
Pain with intrauterine device (IUD) insertion is very common and there are few options for patients to help reduce this pain. Transcutaneous electric nerve stimulators (TENS) are a non-invasive procedure that may help reduce the pain with IUD insertions. The investigators hope that the information gleaned from this study will result in pain control options for future patients who desire an IUD placement.
Primary Outcome
The VAS score is a score of 0-10 with 0 being no pain and 10 being the worse pain imaginable
Interventions
- DEVICE Transcutaneous electrical nerve stimulation (TENS)
- DEVICE Placebo Transcutaneous electrical nerve stimulation (TENS)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2024-06-05 |
| Est. Completion | 2025-02-07 |
| Phase | NA |
What the finished NCT06335823 record still lists
NCT06335823 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).
The record links to 0 conditions, and to 2 interventions - of which Transcutaneous electrical nerve stimulation (TENS) is the first listed.
NCT06335823 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT06335823 about?
NCT06335823 is a clinical study titled "Efficacy of Transcutaneous Electrical Nerve Stimulation (TENS) for Pain Reduction During Intrauterine Device (IUD) Insertion in Outpatient Gynecology". Pain with intrauterine device (IUD) insertion is very common and there are few options for patients to help reduce this pain. Transcutaneous electric nerve stimulators (TENS) are a non-invasive procedure that may help reduce the pain with IUD insertions. The investigators hope that the information g...
What is the current status of trial NCT06335823?
This trial is currently completed. It is a NA study. The enrollment target is 60 participants. The study started on 2024-06-05. Estimated completion is 2025-02-07.
What interventions are being tested in trial NCT06335823?
The interventions under investigation include: Transcutaneous electrical nerve stimulation (TENS) (DEVICE), Placebo Transcutaneous electrical nerve stimulation (TENS) (DEVICE).
Who is sponsoring clinical trial NCT06335823?
This trial is sponsored by University Hospitals Cleveland Medical Center, which has 230 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT06335823's enrollment target sits among peer trials
60 1164th of 2000 higher than 745 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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